UPPER Rapid Quantitative Determination for whole range C-Reactive Protein (hs-CRP+CRP) by DIGFA Method - Indonesia BPOM Medical Device Registration
UPPER Rapid Quantitative Determination for whole range C-Reactive Protein (hs-CRP+CRP) by DIGFA Method is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305320806. The device is manufactured by SHANGHAI UPPER BIOTECH PHARMA CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GOLDEN MEDIKA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHANGHAI UPPER BIOTECH PHARMA CO., LTD.Country of Origin
China
Authorized Representative
PT. GOLDEN MEDIKA MANDIRIAR Address
Jl. Raya Kalirungkut 27 Blok C-65
Registration Date
Apr 20, 2023
Expiry Date
Jan 01, 2025
Product Type
Immunological Test System
C-reactive protein immunological test system.
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